PROTECTIVE FILM - ANVISA Registration 80673850004

Access comprehensive regulatory information for PROTECTIVE FILM in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80673850004 and manufactured by EUROFARM S.P.A. The registration is held by MEDICALL FARMA DISTRIBUIDORA DE PRODUTOS E SERVICOS PARA SAUDE LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including CREMER S/A, CONVATEC, INC., and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.